Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 245075Erstellt: 25. Oktober 2026

Diisopropylethylamine → 2-Chloro-4-[[(1R,2S)-2-hydroxycyclohexyl]amino]-3-methyl-benzonitrile

https://huagongshe.com/reaction/245075

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
Edukt(1S,2R)-2-aminocyclohexan-1-ol hydrochlorideHCID 17039400—
Edukt2-Chloro-4-fluoro-3-methylbenzonitrileHCID 44550971—
LösungsmittelDichloromethaneHCID 6344—
Produkt2-Chloro-4-[[(1R,2S)-2-hydroxycyclohexyl]amino]-3-methyl-benzonitrileHCID 8669378429,6%

Reaktionsschritte

A mixture of 2-chloro-4-fluoro-3-methyl-benzonitrile (500 mg, 2.95 mmol), diisopropylethylamine (1.29 mL, 7.37 mmol), and (1S,2R)-2-aminocyclohexanol hydrochloride (670 mg, 4.42 mmol, Acros®) is microwaved using a CEM® microwave at 190° C. for 2 h and 180° C. for 4 h. The mixture is diluted with dichloromethane and washed with 1 N HCl. The aqueous layer is extracted again with dichloromethane. The combined organic phases are dried over sodium sulfate, filtered, and concentrated in vacuo. The resulting residue is purified using radial chromatography, eluting with 2% methanol/dichloromethane. The isolated product is recrystallized with ether and hexane to yield the title compound as a white solid (231 mg, 29%). LC-ES/MS m/z 265.0 (M+1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08658693B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-7392c902ed19404883235588542a6b88
Quellennotizuspto-grants-2014_02